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Clinical Research Associate (CRA) Training

Clinical Research Associate (CRA) Training
from 4 to 360h flexible workload
valid certificate in your country

What will I learn?

This focused Clinical Research Associate (CRA) Training builds hands-on skills for confident, rule-following trial monitoring. Learn ICH-GCP informed consent rules, key regulatory files, site file setup, drug tracking, protocol issues, source data checks and eCRF methods, serious adverse event management, CAPA creation, visit processes, and readiness for audits in cancer and other studies.

Elevify advantages

Develop skills

  • Master ICH-GCP and IRB basics to conduct compliant trials swiftly.
  • Monitor oncology studies by checking data, handling queries, and ensuring patient safety.
  • Manage protocols and drug supplies by tracking deviations, dosing, and accountability.
  • Oversee informed consent processes with version control, re-consent, and IRB updates.
  • Create CAPA plans and reports to record issues, spot trends, and improve site performance.

Suggested summary

Before starting, you can change the chapters and workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.
Workload: between 4 and 360 hours

What our students say

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EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company where I work.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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